AI Article Synopsis
- The paper outlines a straightforward method for producing a chiral compound, [2.2]paracyclophane-4-thiol, using a specific chiral sulfoxide.
- It highlights a significant achievement in synthetic chemistry by reporting the first successful creation of an enantiomerically enriched planar chiral benzothiazole.
- The research emphasizes the importance of stereochemistry in synthesizing complex organic molecules with specific orientations.
Article Abstract
This paper describes a simple route to enantiomerically enriched [2.2]paracyclophane-4-thiol via the stereospecific introduction of a chiral sulfoxide to the [2.2]paracyclophane skeleton. The first synthesis of an enantiomerically enriched planar chiral benzothiazole is also reported.
Download full-text PDF |
Source |
|---|---|
| http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2686273 | PMC |
| http://dx.doi.org/10.3762/bjoc.5.9 | DOI Listing |
Publication Analysis
Top Keywords
enantiomerically enriched
8
enantiospecific synthesis
4
synthesis [22]paracyclophane-4-thiol
4
[22]paracyclophane-4-thiol derivatives
4
derivatives paper
4
paper describes
4
describes simple
4
simple route
4
route enantiomerically
4
enriched [22]paracyclophane-4-thiol
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!